@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_head {
  this: np:hasAssertion dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion;
    np:hasProvenance dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance;
    np:hasPublicationInfo dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion a np:Assertion .
  
  dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance a np:Provenance .
  
  dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0149925 a ncit:C7057 .
  
  dgn-gda:DGN5ed09dbed5dc4bd950ba5d4d523d4bf4 sio:SIO_000628 miriam-gene:324, lld:C0149925;
    a sio:SIO_001121 .
}

dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance {
  dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion dcterms:description
      "[Seven cases were informative for both genes, loss of heterozygosity occurred for both genes in five, one retained heterozygosity for both, and one SCLC had loss of heterozygosity for APC but not for MCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:1348017;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:44+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}